WO2010028802A1 - Individualisation de moyens auxiliaires médicaux - Google Patents

Individualisation de moyens auxiliaires médicaux Download PDF

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Publication number
WO2010028802A1
WO2010028802A1 PCT/EP2009/006507 EP2009006507W WO2010028802A1 WO 2010028802 A1 WO2010028802 A1 WO 2010028802A1 EP 2009006507 W EP2009006507 W EP 2009006507W WO 2010028802 A1 WO2010028802 A1 WO 2010028802A1
Authority
WO
WIPO (PCT)
Prior art keywords
user
medical
consumables
medical device
housing
Prior art date
Application number
PCT/EP2009/006507
Other languages
German (de)
English (en)
Inventor
Ahmet Konya
Hans-Juergen Kuhr
Original Assignee
Roche Diagnostics Gmbh
F. Hoffmann-La Roche Ag
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Roche Diagnostics Gmbh, F. Hoffmann-La Roche Ag filed Critical Roche Diagnostics Gmbh
Priority to US13/063,113 priority Critical patent/US20110173024A1/en
Publication of WO2010028802A1 publication Critical patent/WO2010028802A1/fr

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Classifications

    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
    • A61B5/00—Measuring for diagnostic purposes; Identification of persons
    • A61B5/15—Devices for taking samples of blood
    • A61B5/151—Devices specially adapted for taking samples of capillary blood, e.g. by lancets, needles or blades
    • A61B5/15146—Devices loaded with multiple lancets simultaneously, e.g. for serial firing without reloading, for example by use of stocking means.
    • A61B5/15148—Constructional features of stocking means, e.g. strip, roll, disc, cartridge, belt or tube
    • A61B5/15178—Stocking means comprising separate compartments or units for new and for used piercing elements
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
    • A61B5/00—Measuring for diagnostic purposes; Identification of persons
    • A61B5/145—Measuring characteristics of blood in vivo, e.g. gas concentration, pH value; Measuring characteristics of body fluids or tissues, e.g. interstitial fluid, cerebral tissue
    • A61B5/14532—Measuring characteristics of blood in vivo, e.g. gas concentration, pH value; Measuring characteristics of body fluids or tissues, e.g. interstitial fluid, cerebral tissue for measuring glucose, e.g. by tissue impedance measurement
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
    • A61B5/00—Measuring for diagnostic purposes; Identification of persons
    • A61B5/15—Devices for taking samples of blood
    • A61B5/150007—Details
    • A61B5/150015—Source of blood
    • A61B5/150022—Source of blood for capillary blood or interstitial fluid
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
    • A61B5/00—Measuring for diagnostic purposes; Identification of persons
    • A61B5/15—Devices for taking samples of blood
    • A61B5/150007—Details
    • A61B5/150763—Details with identification means
    • A61B5/150786—Optical identification systems, e.g. bar codes, colour codes
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
    • A61B5/00—Measuring for diagnostic purposes; Identification of persons
    • A61B5/15—Devices for taking samples of blood
    • A61B5/151—Devices specially adapted for taking samples of capillary blood, e.g. by lancets, needles or blades
    • A61B5/15146—Devices loaded with multiple lancets simultaneously, e.g. for serial firing without reloading, for example by use of stocking means.
    • A61B5/15148—Constructional features of stocking means, e.g. strip, roll, disc, cartridge, belt or tube
    • A61B5/15157—Geometry of stocking means or arrangement of piercing elements therein
    • A61B5/15165—Piercing elements stocked in or on a strip
    • A61B5/15169—Characterized by a rolled strip
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
    • A61B5/00—Measuring for diagnostic purposes; Identification of persons
    • A61B5/15—Devices for taking samples of blood
    • A61B5/151—Devices specially adapted for taking samples of capillary blood, e.g. by lancets, needles or blades
    • A61B5/15146—Devices loaded with multiple lancets simultaneously, e.g. for serial firing without reloading, for example by use of stocking means.
    • A61B5/15148—Constructional features of stocking means, e.g. strip, roll, disc, cartridge, belt or tube
    • A61B5/15157—Geometry of stocking means or arrangement of piercing elements therein
    • A61B5/15165—Piercing elements stocked in or on a strip
    • A61B5/15171—Characterized by propelling the piercing element perpendicular to the direction of movement of the strip
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
    • A61B5/00—Measuring for diagnostic purposes; Identification of persons
    • A61B5/15—Devices for taking samples of blood
    • A61B5/151—Devices specially adapted for taking samples of capillary blood, e.g. by lancets, needles or blades
    • A61B5/15146—Devices loaded with multiple lancets simultaneously, e.g. for serial firing without reloading, for example by use of stocking means.
    • A61B5/15182—Means for keeping track or checking of the total number of piercing elements already used or the number of piercing elements still remaining in the stocking, e.g. by check window, counter, display
    • G—PHYSICS
    • G16—INFORMATION AND COMMUNICATION TECHNOLOGY [ICT] SPECIALLY ADAPTED FOR SPECIFIC APPLICATION FIELDS
    • G16H—HEALTHCARE INFORMATICS, i.e. INFORMATION AND COMMUNICATION TECHNOLOGY [ICT] SPECIALLY ADAPTED FOR THE HANDLING OR PROCESSING OF MEDICAL OR HEALTHCARE DATA
    • G16H20/00—ICT specially adapted for therapies or health-improving plans, e.g. for handling prescriptions, for steering therapy or for monitoring patient compliance
    • G16H20/10—ICT specially adapted for therapies or health-improving plans, e.g. for handling prescriptions, for steering therapy or for monitoring patient compliance relating to drugs or medications, e.g. for ensuring correct administration to patients
    • G16H20/17—ICT specially adapted for therapies or health-improving plans, e.g. for handling prescriptions, for steering therapy or for monitoring patient compliance relating to drugs or medications, e.g. for ensuring correct administration to patients delivered via infusion or injection
    • G—PHYSICS
    • G16—INFORMATION AND COMMUNICATION TECHNOLOGY [ICT] SPECIALLY ADAPTED FOR SPECIFIC APPLICATION FIELDS
    • G16H—HEALTHCARE INFORMATICS, i.e. INFORMATION AND COMMUNICATION TECHNOLOGY [ICT] SPECIALLY ADAPTED FOR THE HANDLING OR PROCESSING OF MEDICAL OR HEALTHCARE DATA
    • G16H40/00—ICT specially adapted for the management or administration of healthcare resources or facilities; ICT specially adapted for the management or operation of medical equipment or devices
    • G16H40/40—ICT specially adapted for the management or administration of healthcare resources or facilities; ICT specially adapted for the management or operation of medical equipment or devices for the management of medical equipment or devices, e.g. scheduling maintenance or upgrades
    • G—PHYSICS
    • G16—INFORMATION AND COMMUNICATION TECHNOLOGY [ICT] SPECIALLY ADAPTED FOR SPECIFIC APPLICATION FIELDS
    • G16H—HEALTHCARE INFORMATICS, i.e. INFORMATION AND COMMUNICATION TECHNOLOGY [ICT] SPECIALLY ADAPTED FOR THE HANDLING OR PROCESSING OF MEDICAL OR HEALTHCARE DATA
    • G16H40/00—ICT specially adapted for the management or administration of healthcare resources or facilities; ICT specially adapted for the management or operation of medical equipment or devices
    • G16H40/60—ICT specially adapted for the management or administration of healthcare resources or facilities; ICT specially adapted for the management or operation of medical equipment or devices for the operation of medical equipment or devices
    • G16H40/63—ICT specially adapted for the management or administration of healthcare resources or facilities; ICT specially adapted for the management or operation of medical equipment or devices for the operation of medical equipment or devices for local operation
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
    • A61B5/00—Measuring for diagnostic purposes; Identification of persons
    • A61B5/15—Devices for taking samples of blood
    • A61B5/150007—Details
    • A61B5/150358—Strips for collecting blood, e.g. absorbent
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
    • A61B5/00—Measuring for diagnostic purposes; Identification of persons
    • A61B5/15—Devices for taking samples of blood
    • A61B5/150007—Details
    • A61B5/150374—Details of piercing elements or protective means for preventing accidental injuries by such piercing elements
    • A61B5/150381—Design of piercing elements
    • A61B5/150412—Pointed piercing elements, e.g. needles, lancets for piercing the skin
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
    • A61B5/00—Measuring for diagnostic purposes; Identification of persons
    • A61B5/15—Devices for taking samples of blood
    • A61B5/150007—Details
    • A61B5/150374—Details of piercing elements or protective means for preventing accidental injuries by such piercing elements
    • A61B5/150381—Design of piercing elements
    • A61B5/150503—Single-ended needles
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
    • A61B5/00—Measuring for diagnostic purposes; Identification of persons
    • A61B5/15—Devices for taking samples of blood
    • A61B5/151—Devices specially adapted for taking samples of capillary blood, e.g. by lancets, needles or blades
    • A61B5/15101—Details
    • A61B5/15103—Piercing procedure
    • A61B5/15107—Piercing being assisted by a triggering mechanism
    • A61B5/15113—Manually triggered, i.e. the triggering requires a deliberate action by the user such as pressing a drive button
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
    • A61B5/00—Measuring for diagnostic purposes; Identification of persons
    • A61B5/15—Devices for taking samples of blood
    • A61B5/151—Devices specially adapted for taking samples of capillary blood, e.g. by lancets, needles or blades
    • A61B5/15101—Details
    • A61B5/15115—Driving means for propelling the piercing element to pierce the skin, e.g. comprising mechanisms based on shape memory alloys, magnetism, solenoids, piezoelectric effect, biased elements, resilient elements, vacuum or compressed fluids
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
    • A61B5/00—Measuring for diagnostic purposes; Identification of persons
    • A61B5/15—Devices for taking samples of blood
    • A61B5/157—Devices characterised by integrated means for measuring characteristics of blood

Definitions

  • the invention relates to a method for upgrading medical aids.
  • EP 1 279 365 describes a possibility for providing a glucose meter with an additional surrounding housing which does not affect the functions of the glucose meter, but gives the patient a better grip or different coloring as well as additional information for the system and to provide it to the patient. Disadvantage of this additional Umgeophuses is that the user has no way to influence the design of this Umgeophuses.
  • This object is achieved by a method for upgrading a medical aid for the treatment of diabetes in the home monitoring area with the following steps: Providing consumables in a housing with a type-specific identification code for use in a medical device,
  • Design of a supplementary module for the medical device Generating a job for the delivery of a supplementary module based on the selection of the user.
  • an application is also applicable to other home-monitoring patients, for example, who often have to determine their coagulation value or control their urine value, which is why the application is not limited to diabetes.
  • the user is given the opportunity of collecting a loan in the form of a recognition code to be able to independently and individually put together additional supplementary modules for medical aids. It is completely independent, by which consumables he has this loan, which he can gain, for example, by adding different recognition codes, by purchasing consumables.
  • the procedure offers the user the possibility of the loan in the form of
  • Supplementary module that, for example, an additional large display to display measured glucose levels facilitates the handling of his illness. In this way, through the individualization, a better management of the patient of his illness can be achieved.
  • the claimed method likewise represents a possibility of individualization for the user, wherein in this embodiment the user can individually design a supplementary module in the form of a housing for an already independently functioning medical aid.
  • a medical device such as a lancing device or an analyzer, which is self-sufficient, d. H. All the functions necessary to perform, for example, a blood glucose measurement or a dose of insulin are available.
  • the individualization process allows the user to retrospectively design this medical device in such a way that it suits his individual requirements.
  • Such an independent functional module that can be supplemented by an additional housing to introduce additional functions in the system is already described in EP 1 967 139 in the form of a collated lancing device.
  • Both methods described here is the principle of individualization of supplementary modules, such as enclosing or additional components for the medical device, but also to select and customize additional software individually. This can take place by means of a rewarding process in which the user can obtain a loan by purchasing consumables, which he can collect via a recognition code on the consumable and can redeem in the future in the form of a supplemental module for a medical device. In both cases, the user can vary his credit by additional payment.
  • Consumables for example, in the form of a magazine of various consumables such as lancing elements, test elements or insulin, regardless of their amount of consumable interact with the medical aid functionally.
  • a system that includes a medical device that can interact with a magazine and a magazine that contains consumables and is insertable into the medical device.
  • the system is characterized in that the magazine is providable with a different number of consumables in the unused state.
  • the medical aid can be designed so that it automatically determines the number of consumables, eg based on the recognition code or another code. This information can be displayed to the user as well as stored and edited in a data storage or processing unit.
  • Tape length can be varied in the magazine without the magazine must have a different shape or size.
  • the housing can be the same size with a magazining between 1 and about 400 lancets.
  • This principle of tape-shaped magazining can be used not only for piercing elements but also, for example, for test elements, integrated lancets with test elements or other magazineable consumables. This ensures that, for example, the design of a Umgeophuses does not have to be adapted to the independently functioning lancing device with integrated magazine with different amount of lancing elements in size. As a result, a more cost-effective provision of very differently designed enclosures is made possible in addition. Consequently, the embodiment of the described system offers a possibility of implementing an individualization method as described above.
  • the preferred system can always interact with the same medical device regardless of the amount of consumables, different levels of magazine filling can be provided without the user needing another medical device. This can be achieved due to a uniform size of the magazine, regardless of the number or amount of consumable.
  • an adaptation module can be provided which is attached either to the magazine or to the magazine medical aids to attach different sized magazines in the same receiving location of the tool can. The functionality of the magazine and medical device is not affected. In this case, the amount of credit stored in the recognition code can either increase linearly with the amount of consumable or increase disproportionately, eg faster with a larger amount of supplied consumable per magazine.
  • the revaluation or individualization method according to the invention can be carried out with the aid of a computer program which is made available either on a data medium such as a CD-ROM, USB stick or floppy disk, or via a network, for. B. accessible via the Internet for the user.
  • a computer program which is made available either on a data medium such as a CD-ROM, USB stick or floppy disk, or via a network, for. B. accessible via the Internet for the user.
  • the user is provided, for example, an input mask into which he can enter the required data, such as recognition code and / or user identification, using these data to get displayed a selection of products that his user status, the the information of the recognition code and / or the user identification has been determined corresponds.
  • required data such as recognition code and / or user identification
  • the program may have a variety of ways in which the selection is presented to the user.
  • An alternative is that the user gets generated various selection displays based on a recognition code with his user identification.
  • Another alternative is that the user can generate a fictitious selection of user states that interest him. This gives the user the opportunity to look at product combinations that interest him, but he can not afford them with his current loan. This can motivate him to increase his credit and thus achieve a better state of his disease surveillance and therapy.
  • the program also offers the possibility to store personal data and loan amounts, which will be implemented later in the form of a delivery.
  • the user can also access all stored products (in the form of
  • Supplementary modules to decide whether to add more recognition codes to get more choices.
  • the user identification can optionally be included or neglected for the selection of the displayed products.
  • the user is given the opportunity to design his choice into a task that results in the delivery of the selected supplementary module.
  • Insulin pumps (Accu-Chek ® Spirit®), data processing equipment (Accu-Chek® Smart Pix®), can be individually expanded and / or designed according to his taste and requirements.
  • the input module has a possibility to enter a fictitious recognition code or to display products for different user states without having actually acquired a recognition code.
  • a medical device As a medical device, all analysis equipment, lancing devices, data processing systems, insulin pump systems, continuous measuring devices, as well as any utensils that a user in the home monitoring area used to treat his illness, are considered.
  • These medical aids are preferably equipped with consumables, the consumable can be provided with a recognition code or directly on purchase of the consumable can lead to a selection by the patient of a supplementary module, for example in the form of a housing for the medical device.
  • the medical aid is preferably already functional without the supplementary module and can be upgraded or individualized by a supplementary module.
  • the supplementary module can also be a medical tool here. This can also be self-sufficient.
  • the medical device is suitable for the analysis or therapy of a diabetic and may be a receiving location for one or more
  • Consumables contain and at least one consumable that can be inserted into the receiving station, the consumable having a recognition code.
  • the aid can include a readout unit which is designed to read the recognition code on the consumable furthermore in a data storage and data processing unit which is designed to add different recognition codes and / or to provide a recognition unit. Code to combine with a user code. This makes it possible to determine user-specific data, which can lead, for example, in a database for the selection of specific modules or supplementary modules with certain configurations.
  • the medical device may include means for signaling a sufficient score to upgrade the system.
  • This device may have an acoustic, graphic or haptic design.
  • the recognition code or several recognition codes together and / or a recognition code can be combined with the user code to determine whether a sufficient score has been reached, which was predetermined either by the user or the system , For example, if the user desires a particular supplemental module, a threshold may be set beyond which the resource signals that this score has been reached.
  • the score can be compared with scores in a database for supplemental modules and the user can be shown on the medical device which selection of supplemental modules would be eligible for that score.
  • a unit can be provided, which allows the tool to automatically transmit this score to a central database as soon as the aid is linked with this database for data exchange.
  • the connection of the medical device with the database can take place via cable connections or wireless via infrared, radio or bluethooth interface.
  • the recording of the connection with the database can be done automatically by the tool itself, which can be triggered either by reaching a certain reading or a certain number of measurements, or by reaching a certain score.
  • the tool may include acoustic, graphical or haptic means to communicate various states to the user. This can be, for example, a measurement result of a measurement, or exceeding a threshold value either by a measurement signal or a score. Other states, such as the battery status or other device functions can be displayed to the user via this display means.
  • the medical device can be configured with a sensor that immediately detects when inserting the consumable, whether it is a newly inserted consumables or an already at least partially consumed consumables. The amount of consumed or not yet consumed consumables can be displayed. In this way it is prevented that a previously used consumable is used again to revalue the score.
  • the medical device may have a device that makes it possible to change the recognition code so that when re-inserting or inserting the same consumable in another medical device immediately recognized that this consumable has already been detected and registered once. This can be done for example by a laser irradiation, wherein the laser can also be used to read a code. It could also be a mechanical marking that changes or destroys at least parts of the recognition code.
  • the consumables may be in the form of lancing elements such as lancets, analytical test elements, catheters, insulin cartridges or other utensils needed by a diabetic to treat his diabetes associated with a medical device.
  • lancing elements such as lancets, analytical test elements, catheters, insulin cartridges or other utensils needed by a diabetic to treat his diabetes associated with a medical device.
  • the design of these consumables is not limited and can be any form or functionality, such widely known in the art, suppose. For example, multiple uses may also be used. Preferably, however, these are disposable units.
  • the consumables are preferably housed in a housing, such as a magazine or a storage container. These can also be plastic or glass cartridges for storing liquids.
  • the consumables can either be removed individually and interact with the aid or, when a magazine is used, interact directly with the aid in magazine form so that provision of the consumable by the aid can be carried out directly using the medical aid.
  • a consumable can also be considered any additive for the medical device, such. an additional housing or other supplementary modules for the medical device.
  • the surrounding housing interacts with the medical device so that it surrounds it at least in part. In this way, both the appearance, but also the functional scope of the medical device can be changed.
  • medical aids such as lancing devices, analyzer and insulin pumps do not have an infinite lifetime, they can also be regarded as consumables within the meaning of the invention, and consequently be provided with a recognition code. In this particular case, the medical aid is also the consumable.
  • the consumable or the magazine with consumables can be designed so that it always has the same size regardless of the number of consumables to be introduced into the receiving location of the medical device.
  • supplementary module is understood to be any additional element which may be useful to the user in the management of his illness.
  • These may be components that may be used independently of the medical device or that may directly receive a mechanical or electronic connection with the medical device. For example, they may be attached to or in addition to the normal functioning of the medical device on the medical device be activated or implemented, or interact with the medical device in any form. Interaction can be understood as meaning all mechanical or electronic interactions between the medical device and the supplementary module.
  • the add-on module may be either a hardware module (e.g., enclosures with or without additional features, a pocket, grips), but also a software module.
  • the software module may already be implemented on the medical device but may not yet be activated when the device is purchased and be enabled directly on the medical device by providing the identification code.
  • the supplementary module can be activated by electronic transmission of the identification code to a control center or database which, in connection with the user identification, enables the feature electronically. This activation can be done by transmitting a further code to the user, who enters this in the medical device, but it can also be done directly electronically on the tool, if this is designed to.
  • Another alternative way to make the transfer of codes and orders is the transmission via mobile phone or similar electronic devices that have a send function.
  • the medical device need only have an interface with the transmitter to transmit the code or order. This can be done for example via a normal hardware interface such as USB or via a Bluetooth or infrared interface.
  • the supplementary module is in a preferred embodiment, a surrounding housing, which may contain both design and functional components. However, it may also be additional supplemental modules such as a flashlight, a laser pointer or a USB stick that can interact with the medical device in a modular or functional manner. Further supplementary modules that do not interact directly with the medical device are an extension to a storage space eg for test elements or a supplement to a display device or a display. Preferably, however, the enclosure is provided with additional supplemental modules, which constitute an additional functional component for the medical device. For example, this group includes
  • the identification code which may be on, on or in the various types of consumables, may be any form of pictorial or electronic representation of information.
  • the identification code may also contain information about the type of consumable and its quantity. Examples of these are optical or electronic barcodes, code numbers, glued-on points or other means that can be read by the user or electronic aids in optical or electronic form. In the case of the electronic readout, this can be ensured by an additional device or by the device into which the consumables are introduced.
  • the further processing e.g. in the form of storage of the recognition code can either be purely mechanical by the user by the glued images, for example. In the form of points, transfers to a form with which he then makes an order. Alternatively, it can also be a direct transfer to a computer or a by a coupling of the medical aid, which has stored the recognition codes
  • the Finishing device which may be either the medical device itself or a computer, but also a database or an input program, the recognition code is at least temporarily stored and processed.
  • This further processing may also include the steps of combining user identification (if any) and / or providing a selection of products.
  • the recognition code contains credit information that allows the user to use this code to order supplemental medical device kits.
  • the information of various recognition codes can be combined with one another, and thus can lead to a different or extended selection for the supplementary modules for the user.
  • the recognition code may be used in conjunction with a user identification to provide a selection of at least one embodiment of a medical aid supplement module.
  • the user information can only one
  • User recognition e.g. in the form of the name or a recognition number or other information.
  • this user identification can be an information (for example identification or type name of a device) for the medical aid.
  • personal data may be added as a user identification, for example, the age of the user, certain preferences of the user, knowledge of previously used devices or utensils by the user or other personal data to be.
  • this user identification may additionally contain information about the disease state of the user, so that this information is used together with the recognition code to provide a more differentiated selection for the user in the selection program.
  • This disease state information can be, for example, in the field of diabetes, information about whether the user is a Type 1 or Type 2 diabetes patient, whether he is insulin dependent or not insulin dependent, which systems he has been using used and what other diseases he has.
  • the selection program is in the form of a catalog, for example, such disease-related information can be limited, but it is also possible here to differentiate between potentially useful supplementary modules for different disease groups such as type 1 diabetes and type 2 diabetes, since the type 1 diabetic usually insulin-dependent, while the type 2 diabetic patient does not yet have to be.
  • the selection for the type 2 diabetic patient would not be offered all utensils in the form of supplement modules from the insulin pump area, unless at his special request.
  • the user can select both design and functional components when choosing a supplemental module.
  • the design components include above all:
  • Haptic e.g., surface texture
  • the functional components are used primarily to make an individualization for the supplementary module and thus also for the devices. This is to get a better identification of the user with his utensils in connection with his illness. This is intended to increase the user's awareness of the correct behavior in dealing with his illness. This includes regular determination of the level of glucose in the blood for the diabetic, or the better therapeutic setting by insulin.
  • the functional components can be:
  • System or device can be functionally coupled.
  • Additional consumables such as lancing elements, test elements, etc.
  • Variation of the size of the supplementary module for the adapted handling of the medical device eg in the case of the visually impaired or older people.
  • Additional surrounding housing to introduce additional functions into the medical device such as
  • FIG. 1 DESCRIPTION OF THE FIGURES FIG. 1:
  • FIG. 2 is a diagrammatic representation of FIG. 1
  • FIG. 3 Schematic representation of an individualization process for a surrounding housing FIG. 3:
  • FIG. 1 schematically shows the sequence of the method steps for upgrading a medical aid.
  • a consumable (1) shown in this example as a magazine for test elements or for lancets (3), provided first.
  • a recognition code (2) is mounted, which is stored together with the user identification (4) on a data processing device (eg a computer, a database or an Internet server), or is noted by the user on a form.
  • a data processing device eg a computer, a database or an Internet server
  • a user status is electronically or manually from a series of stored or printed user states (1, 2, 3... X) by means of the recognition code (2) and the user identification (4) certainly. Because of this user status, the user is offered various choices for selecting a supplemental module. This can be done in the form of a list of product names together with the necessary credit to obtain this supplementary module, or alternatively, a visual representation of the various supplementary modules can take place, which is particularly important for the design of the
  • Supplementary module makes sense.
  • the user may select a combination of different components of the supplementary module, e.g. combine the color with a specific pattern as well as additional functions for a supplementary module.
  • the user can be displayed at any time the necessary amount of credit for its combination and compared with the entered recognition code or user status.
  • a delivery order based on his selection. This can be done using an electronic selection module in the form of an electrical order or catalog as a selection module in the form of a delivery order through a form on which the necessary data such as identification code and user identification were entered.
  • FIG. 2 shows three different embodiments of a surrounding housing (30a, 30b, 30c), which differ from one another on account of their functionality or configuration.
  • the surrounding housing may have various additional elements (31), as shown for example for the surrounding housing (30b) in the form of a display (31) or alternatively the surrounding housing (30c) Additional element (31) in the form of a USB interface has.
  • This is intended to exemplify the provision of a selection of design or functional properties of a housing for a self-contained medical device as would be a lancing device in this case (which is not shown here).
  • This surrounding housing (30a, 30b, 30c) can, for example, furthermore comprise a housing wall (32), a trigger (34), an interface (36) and a drive (39).
  • this selection is registered, this can be done by recording the selection by the user in a form or, preferably, by the selection program on a computer or in a database. Based on this registration, an order to deliver the selected supplemental module can then be generated if the user so wishes.
  • a user identification for example in the form of an address or a user identifier, is also required here in order to provide the user with his selected supplementary model.
  • FIG. 2 selection options for a surrounding housing, shown by way of example in FIG. 2, are possible as already described under FIG. 1 both in electronic and in written form.
  • the possibilities of displaying various design as well as functional components can be presented in an electronic data processing program or a database much easier and more convenient for the user.
  • FIG. 3 shows a consumable (1) in the form of a magazine for, for example, lancets or test elements.
  • the lancets or test elements are mounted on a belt (18), which is moved by a drive mechanism (15) to the puncture position and has a further drive mechanism (1 1) for advancing the tape to move to the next consumable.
  • a special feed mechanism regardless of the number of consumables (1) such as test elements or lancets, the same magazine shape and size can be made.
  • the surrounding housing (3) does not have to be additionally adapted to the size of the lancing device or test element magazine, but a universal size must be provided at least for the receiving position in the form of a recess (31) can. This leads to a

Abstract

L'invention concerne un procédé d'évaluation d'un moyen auxiliaire médical pour le traitement du diabète dans le domaine de la surveillance à domicile, comprenant les étapes: préparation du consommable dans un logement avec un code de reconnaissance spécifique au type pour l'utilisation d'un moyen auxiliaire médical, mise en mémoire d'un code de reconnaissance conjointement avec une identification d'utilisateur et détermination d'un état d'utilisateur, offre d'un choix, qui correspond à l'état d'utilisateur, d'au moins une configuration d'un module complémentaire pour le moyen auxiliaire médical, génération d'un ordre de livraison d'un module complémentaire en raison du choix de l'utilisateur.
PCT/EP2009/006507 2008-09-09 2009-09-08 Individualisation de moyens auxiliaires médicaux WO2010028802A1 (fr)

Priority Applications (1)

Application Number Priority Date Filing Date Title
US13/063,113 US20110173024A1 (en) 2008-09-09 2009-09-08 Individualization of medical adjuvants

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
EP08015878A EP2160979A1 (fr) 2008-09-09 2008-09-09 Individualisation de moyens d'aide médicaux
EP08015878.5 2008-09-09

Publications (1)

Publication Number Publication Date
WO2010028802A1 true WO2010028802A1 (fr) 2010-03-18

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US (1) US20110173024A1 (fr)
EP (1) EP2160979A1 (fr)
WO (1) WO2010028802A1 (fr)

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US20110173024A1 (en) 2011-07-14

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